EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

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EnhancerAtlas ID
HS048-37799 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:114360160-114361610 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr9:114360676-114360693GGGGACACGGTGACCTG+6.41
ESR2MA0258.2chr9:114360677-114360692GGGACACGGTGACCT-7.08
Enhancer Sequence
AGATAGAAGT CCATGCACCT CTTTCAGATG GAAACAGCCA CGCATTTCAA GGCAGTCTCA 60
GAACTCCTGA AAACCACCGG AGGGCGCCGC TGCTCCGCCC CATTTTCAGG TGCGTTTTTT 120
TTTTTTTTAA ATACTTTTTT TTCTCTCTTT TCTTGTAGAG AGGAGCCTCA CTGTGTTGCC 180
TAGGCGATCC GCCCGCCTCG GTCTCCCAAA GTGCTGGGAT TACAGGTGTG AACCACTTGC 240
ACTCAGCCAT CGGGTGCGAA TTTTCTTTGG CCCAGTAGGG ATTTGAGTTT AAACTCCACA 300
CCAAACCGAT TTTGAGCTGA AACGCTGCAC CAAAGCAAGG GAAGATGATG AAGGCTGCCC 360
CGAGCTGGGG GTTCAGGATG TTCTGCTTGG ACTGAACTCT GCCGAATCAC TTGGGACCTG 420
CGCCTTCCCG CGGGTGCATC CGCTACAAAC AATCCAGTTA CGAAACCATT TGGAGCTGCC 480
AGTGATCTCC CCAGCTCCCC TACCGGTGCC GCGGGAGGGG ACACGGTGAC CTGGAGGGAG 540
CACTCCCGCA TTGCGAGGGA GCCAGGGGGG CGGTCTGATC TGCAGCCCGG GGTTGTTCCT 600
TCTTTTCTTT TTTTAAAATT AAGACTTTTT TTGTGACGGA GTCTCGCTCT GTCGCCCAGG 660
CTGAAGTGCA ATGGCGCGAT CTCAGCTCAC TGCAACCTCC GTCTCCCGGG TTCAAGCGGT 720
TCTCCTGTCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCG CCCGCCACCA CGCCCAGCTA 780
ATTTTTGTAC TTTTAGTAGA GACGGGGTTT CCCCATGTTG GCCAGACTGG TCTAGAACTC 840
CTGAGCTCAA ATGATTCGCC CGCCTCGACC TTCCATAGTG CTGGGATTAC AGGCGTGAGC 900
CACCGCGCCA GGCCCTACGT ATCATTTTTA CGGTGAGACA TTTGCAGTTT ACTCTGTTAT 960
TTCGAAATAC ACATTATTGG CTCTAGTCAC TCTGCTGTGC AACAGATCTC AGAACCTACT 1020
CCTCTCGTCT CTGAACTTCG TACCCTTTGG CCAACAAGCC CCCATTCCCC CCCGAACCCG 1080
CTCCCAGCCT CTGGCAACCA TCATTCTAGT CGTTATTTCT ATGAGTTCAA CTTCTTTAGA 1140
GTTCACACAT CTTTGTCCCT TTCCCCAAAA AAGCAACCGC TGGGCTTCCA AACTCGCTAC 1200
AAGTCCAGAA GCCCTCCTGG AAAGGGTCTG GCCGCAGAGG GGCCAGGTCC CGGGAAAGTC 1260
TCGCCCGCCC GAGGAGGGGG CCTGGCGCGG CGCCCGGCCT TTGCCCGCTC GCCCTTTGCT 1320
CCCACCCTCG CCTCCCGCCG CCCGCCGCCC GCTTGCCCAT TCCCGAATCC CCACCCCGAT 1380
CTTTCTTCTT CTACCCTCCC CCAGTTGTGC AGTCCAGCAA GTTCCCTGGC CAGCCCCCTC 1440
CCGGGTGCAG 1450